rs863225017

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;-)	0	common in clinvar

Make rs863225017(-;A)

Make rs863225017(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

31209509

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs863225017
dbSNP (classic)	rs863225017
ClinGen	rs863225017
ebi	rs863225017
HLI	rs863225017
Exac	rs863225017
Gnomad	rs863225017
Varsome	rs863225017
LitVar	rs863225017
Map	rs863225017
PheGenI	rs863225017
Biobank	rs863225017
1000 genomes	rs863225017
hgdp	rs863225017
ensembl	rs863225017
geneview	rs863225017
scholar	rs863225017
google	rs863225017
pharmgkb	rs863225017
gwascentral	rs863225017
openSNP	rs863225017
23andMe	rs863225017
SNPshot	rs863225017
SNPdbe	rs863225017
MSV3d	rs863225017
GWAS Ctlg	rs863225017

Max Magnitude

0

ClinVar
Risk	rs863225017(A;A)
Alt	rs863225017(A;A)
Reference	Rs863225017(-;-)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.31227627dupT
CLNSRC	Quest Diagnostics
CLNACC	RCV000201051.1,